ODRClass 2
Electrosurgical Patient Return Electrode
FDA adverse event reports and recall history for electrosurgical patient return electrode (product code ODR), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 264
- Deaths
- 1
- Injuries
- 105
- Malfunctions
- 134
Reports per year
105
307
9408
11809
2310
611
412
613
414
216
117
226
Source: FDA adverse event reports by year received, 2005–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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